Hereditary Peripheral Neuropathies Gene Mutation Panel, NGS
Vitamin B3 (Niacin)
Huntington Disease Mutation Analysis
Sex Hormone Binding Globulin (SHBG)
Adenosine Deaminase, Body Fluid
Immunoglobulins (IgG, IgA, IgM)
Monoclonal Protein ( M Protein) Study, 24 Hour, Urine
Synovial Sarcoma, SS18 Gene Translocation, RT-PCR, Paraffin
Solute Carrier Family 28 Member 3 (SLC28A3) Genotyping
Coagulation Factor VII Inhibitor Screen, Plasma
LDS
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Congenital Adrenal Hyperplasia (CAH) Profile
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Diseases
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All
Diseases
CPT
LOINC
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Additional ICD10
Congenital Adrenal Hyperplasia (CAH) Profile
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